Synthetic approach to cis and trans-decalins via Diels-Alder reaction and ring-closing metathesis as key steps: further extension to dioxapropellane derivative by ring-closing metathesis

KOTHA, S
CHAVAN, AS
DIPAK, MK

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Publication date

January 2011

DOI

10.1016/j.tet.2010.10.080

Publisher

Elsevier BV

Journal

Tetrahedron

Abstract

9,10-Substituted cis and trans-decalins were synthesized by a simple route using the Diels-Alder reaction and ring-closing metathesis (RCM) as key steps. Later, the cis-decalin system has been extended to 3,8-dioxa[8.4.4]propellane derivative by RCM sequence as a key step. (C) 2010 Elsevier Ltd. All rights reserved

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Synthetic approach to cis and trans-decalins via Diels-Alder reaction and ring-closing metathesis as key steps: further extension to dioxapropellane derivative by ring-closing metathesis

Abstract

Extracted data

Synthetic approach to cis and trans-decalins via Diels-Alder reaction and ring-closing metathesis as key steps: further extension to dioxapropellane derivative by ring-closing metathesis

Abstract

Extracted data

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